| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130372547-130372941 | Common:3; Rare:133 | ||||
| chr2:130836781-130836935 | Common:2; Rare:67 | ||||
| chr2:131093212-131093580 | Common:2; Rare:143 | ||||
| chr2:131105192-131105387 | Common:2; Rare:89 | ||||
| chr2:131492089-131492329 | Common:3; Rare:87 | ||||
| chr2:131492378-131492441 | Common:1; Rare:24 | ||||
| chr2:131492719-131492949 | Common:4; Rare:72 | ||||
| chr2:131493034-131493140 | Common:1; Rare:30 | ||||
| chr2:132416398-132416694 | Common:1; Rare:75 | ||||
| chr2:132416762-132416879 | Common:1; Rare:29 | ||||
| chr2:132417076-132417327 | Common:1; Rare:70 | ||||
| chr2:132670168-132670347 | Common:1; Rare:41 | ||||
| chr2:134918589-134919044 | Common:1; Rare:174 | ||||
| chr2:135052218-135052310 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chr2:135531153-135531629 | Common:1; Rare:106 |